The invention relates to new 3-benzylidene-camphor derivatives of the formula: ##STR1## in which R1 denotes H or SO3.crclbar. M.sym., with M=H, an alkali metal or N.sym. (R3)4, with R3 =H or c1 -c4 alkyl or hydroxyalkyl; R2 denotes c1 -c4 alkyl or c1 -c4 alkoxy and n=0-4; and Z denotes ##STR2## in which R4 has the same meaning as R1 and can be identical or different, or alternatively ##STR3## in which R5 denotes H, optionally substituted aryl, c1 -c4 alkyl, --CN, --C00R7 or ##STR4## and R6 denotes --COOR8 or ##STR5## in which R7 and R8, which are identical or different, denote alkyl, alkenyl, cycloalkyl or aralkyl and R9 and R10, which are identical or different, denote H, alkyl, alkenyl or cycloalkyl; if R5 =H, alkyl or aryl, R6 can represent --COO.crclbar. M.sym. ; the methylidene-camphor radical, on the one hand, and the radical Z, on the other hand, are in the meta or para position. These derivatives act as sun filters.
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1. 3-Benzylidene-camphor derivative having the general formula: ##STR38## in which R1 denotes a hydrogen atom or the radical SO3.crclbar. M.sym., in which M is hydrogen, an alkali metal or the group N.sym. (R3)4, each R3 independently denoting hydrogen or a c1 to c4 alkyl or hydroxyalkyl group; R2 denotes a linear or branched c1 to c4 alkyl radical or a c1 to c4 alkoxy radical, n being 0 or an integer from 1 to 4 such that when n is 2 or more the R2 radicals can be the same or different; and Z represents a group of the formula: ##STR39## in which R5 denotes a hydrogen atom, a c1 to c4 alkyl radical, an aryl radical, an aryl radical substituted by one or more halogen atoms or by c1 to c4 alkyl or alkoxy groups, or a radical ##STR40## and R6 denotes a radical --COOR8 or ##STR41## in which R7 and R8, which are identical or different, denote a substituted or unsubstituted alkyl, alkenyl, cycloalkyl or aralkyl radical containing up to 20 carbon atoms, which substituent is one or more hydroxyl, alkoxy, amine or quaternary ammonium groups, and R9 and R10, which are identical or different, denote a hydrogen atom or a substituted or unsubstituted alkyl, alkenyl, cycloalkyl or aralkyl radical containing up to 20 carbon atoms, which substituent is one or more hydroxyl, alkoxy, amine or quaternary ammonium groups, or, alternatively, if R5 denotes a hydrogen atom, an alkyl radical or a substituted or unsubstituted aryl radical, R6 can also represent a radical --COO.sym. M.crclbar., M being defined as above, with the proviso that the methylidene-camphor radical and the radical Z, which are attached to the aromatic nucleus A, are either in the meta position or in the para position relative to one another.
2. A derivative according to
3. A derivative according to
4. Process for the preparation of a compound as claimed in
5. A composition suitable for cosmetic use which contains at least one 3-benzylidene-camphor derivative as defined in
6. A composition which contains at least one derivative as claimed in
7. A composition according to
8. A composition according to
9. A composition according to
10. A composition according to
11. A composition according to
12. A composition according to
13. Process for protecting the human epidermis against UV-A and/or UV-B rays, which comprises applying thereto at least one derivative as defined in
14. Process for protecting a coloured cosmetic composition against UV radiation, which comprises incorporating therein at least one derivative as defined in
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This is a divisional of application Ser. No. 505,090 filed June 16, 1983, now U.S. Pat. No. 4,585,597.
The present invention relates to compounds derived from 3-benzylidene-camphor, to a process for their preparation and to their use in protection against ultraviolet radiation in the cosmetics field.
It is known that light radiation with wavelengths of between 280 and 400 nm makes it possible to brown the human epidermis and that rays with wavelengths of between 280 and 320 nm, known by the name UV-B can also cause erythema and skin burns, which can hinder the development of a tan.
It is already known to use compounds which are active in the abovementioned wavelength range of 280-320 nm. U.S. Pat. No. 3,781,417 describes 3-(4'-methylbenzylidene)-camphor, the absorption maximum of which is at 297 nm, as a UV-B absorber. This compound has good solubility in oils, but is insoluble in water.
Other benzylidene-camphor derivatives are also known for possessing absorption properties in the wavelength range of 280-320 nm. These include brenzylidene-camphor derivatives containing a quaternary ammonium radical on the benzene nucleus, in the para position relative to the bornylidene radical, according to French Pat. No. 2,199,971, benzylidene-camphor derivatives sulphonated on the methyl radical in the 10-position of the camphor or in the 3'-position or 4'-position on the benzene nucleus, according to French Pat. Nos. 2,282,426 and 2,236,515, and p-methylbenzylidene-camphor derivatives substituted on the p-methyl group, according to French Pat. Nos. 2,383,904, 2,402,647 and 2,421,878.
However, although the UV-B rays with wavelengths of between 280 and 320 nm play a predominant part in the production of solar erythema and must be filtered out, it is no less true that the UV-A rays, with wavelengths of between 320 and 400 nm, which cause the skin to brown, also damage the skin, in particular in the case of a sensitive skin or a skin continually exposed to solar radiation. It has been found that the UV-A rays can potentiate the action of the UV-B rays, as has been described by several groups of authors and more particularly by J. Willis, A. Kligman and J. Epstein (The Journal of Investigative Dermatology, Volume 59, No. 6, page 416, 1973) under the name Photo-enhancement. The UV-A rays favour the initiation of the erythematous reaction or increase this reaction in certain subjects. Likewise, they can be the cause of phototoxic or photoallergic reactions.
Attempts have therefore been made to find compounds which absorb the UV rays strongly over a wide band; and compounds absorbing the UV rays with wavelengths of between 315 and 340 nm, in particular, have been discovered, such as 3-para-hydroxybenzylidene-bornan-2-ones of French Patent Application No. 2,430,938 or 3-cinnamylidene-camphor of U.S. Pat. No. 3,781,417.
Furthermore, it is known that the constituents present in cosmetic preparations, and in particular certain dyestuffs in dyeing compositions, coloured hair lacquers, shampoos, setting lotions and make-up products such as tinted creams, nail varnishes and lipsticks, do not always possess sufficient light stability, and that they degrade under the action of light radiation.
Consequently, it is desirable to have available a group of compounds capable of absorbing both the UV-A rays and the UV-B rays, and to be able to protect the various products sensitive to this radiation by incorporating such agents which filter out the UV-A and UV-B rays into the products, preparations and compositions sensitive to this radiation.
We have discovered that, surprisingly, certain 3-benzylidene-camphor derivatives have good filtering properties with respect to UV-A and UV-B rays, are soluble in the customary cosmetic solvents and have good heat stability and excellent photochemical stability.
The present invention therefore provides 3-benzylidene-camphors of the general formula: ##STR6## in which R1 denotes a hydrogen atom or a radical --SO3- M+, in which M denotes a hydrogen atom, an alkali metal or a group N(R3)4+, R3 denoting a hydrogen atom or a C1 to C4 alkyl or hydroxyalkyl radical, R2 denotes a linear or branched C1 to C4 alkyl radical or a C1 to C4 alkoxy radical, n being 0 or an integer from 1 to 4; and when n is 2 or more R2 radicals can be the same or different; and Z represents a group in which R4 has the same meanings as R1 and can be identical to R1 or different from R1, or alternatively a group ##STR7## in which R5 denotes a hydrogen atom, a C1 to C4 alkyl radical, an aryl radical optionally substituted by one or more halogen atoms or by C1 to C4 alkyl or alkoxy groups, or a radical --CN, --COOR7 or ##STR8## and R6 denotes a group --COOR8 or ##STR9## R7 and R8, which are identical or different, being alkyl, alkenyl, cycloalkyl or aralkyl radicals containing up to 20 carbon atoms, which are optionally substituted by one or more hydroxyl, alkoxy, amine or quaternary ammonium groups, and R9 and R10, which are identical or different, denoting a hydrogen atom or alkyl, alkenyl, cycloalkyl or aralkyl radicals containing up to 20 carbon atoms, which are optionally substituted by one or more hydroxyl, alkoxy, amine or quaternary ammonium groups, or alternatively, if R5 denotes a hydrogen atom, an alkyl radical or an optionally substituted aryl radical, R6 can also represent a radical --COO.crclbar. M.sym., M being defined as above, the methylidene-camphor radical, on the one hand, and the radical Z, on the other hand, being attached to the aromatic nucleus A either in the meta position or in the para position relative to one another.
The following radicals may be mentioned amongst the preferred radicals R7, R8, R9 and R10 : ethyl, propyl, butyl, hexyl, 2-ethylhexyl, menthyl, oleyl, benzyl and 4-methoxybenzyl, and the phenyl radical may be mentioned amongst the preferred aryl radicals for R5.
Depending on the nature of the substituents R1, R2, R4, R5 and R6, the compounds of the formula (I) can be water-soluble or liposoluble.
If Z represents a group ##STR10## and if R6 is different from --COO.crclbar. M.sym., R1 is preferably a hydrogen atom; these compounds are generally lipophilic.
The compounds of the formula (I) have molar absorption coefficients (ε) which are generally high, generally above 30,000 at between 300 and 380 nm.
The position of the absorption maxima for the compounds of the formula (I) depends on the nature of R2 and also on the relative position of the methylene-camphor radical, and the radical Z to one another and also to the group(s) R2 when the latter are electron donors.
In general, the products in which the methylidene-camphor radical and the radical Z are in the para position absorb at wavelengths higher than those at which the corresponding meta-substituted products absorb.
According to the invention, a wide range of compounds is therefore available, constituting sun filters which filter out both the UV-A rays and the UV-B rays.
The present invention also provides a process for the preparation of the compounds of the formula (I).
The compounds of the formula (I) can be obtained by the following processes, which differ according to whether the compounds are symmetrical or asymmetrical.
1--Process for the preparation of the symmetrical compounds of the formula (I) in which Z= ##STR11## and R1 =R4 ##STR12##
This type of reaction can be carried out in an anhydrous solvent, which is preferably aprotic, in the presence of an organic base such as an alkali metal alcoholate, or of a inorganic base such as an alkali metal amide or hydride, the water formed being removed. In certain cases, it is also possible to carry out the reaction in a water-immiscible solvent, in the presence of aqueous solutions of sodium hydroxide or potassium hydroxide.
2--General process for the preparation of the symmetrical and asymmetrical compounds
(a) Z= ##STR13## R4 being identical to R1 or different from R1. ##STR14##
The reaction can be carried out under conditions identical to those described for process (1).
(b) Z= ##STR15##
The reaction scheme used is as follows: ##STR16## It corresponds to the conventional formation of a cinnamic acid derivative from an aromatic aldehyde.
The preferred compounds (I) according to the invention are the compounds in which Z is in the para position, the majority of which constitute sun filters which filter out the UV-A radiation, that is to say filters having an absorption maximum above or equal to 320 nm.
These compounds desirably have the formula: ##STR17##
The compounds of the formula (II) in which Z is in the para position) have very good solubility in water or oils, depending on the nature of the substituents.
Of course, the compounds of the formula (I) or (II) can give rise to "cis-trans" isomerism around one or more double bonds, and all the isomers form part of the present invention.
The compounds of the formula (I) or (II) according to the invention are further illustrated by Examples (1) to (23) which follow, and the characteristics of these compounds: preparative procedure, melting point, wavelength corresponding to the absorption maximum (λ)max, molar absorption coefficient (ε) and analysis, are indicated in the table below.
TBL3 ##STR18## Example R1 n, R2 Z Preparative procedure Melting point UV absorption λmax. (ε) Analysis 1 H O ##STR19## A 258°C 347 nm (CHCl3)(ε = 35,000) Theory: H C:69.68:7.10 S:6.64Found:C:69.96H:7.07 S:6.59 in the para position 2 H O ##STR20## A -- 342 nm (CHCl3) (ε = 39,600) -- in the para position 3 H O ##STR21## C oil 328 nm (EtOH)(ε = 39,000) Theory: C:76.77 H:9.40Found:C:76.76 H:9.34 in the para position 4 H O ##STR22## B 227°C 327 nm (EtOH)(ε = 41,000) Acid number:Theory: 3.22 meq/gFound:3.28 meq/g in the para position 5 H O ##STR23## D 132°C 350 nm (CHCl3)(ε = 50,000) Theory: H C:76.01:6.93 N:3.85Found:C:75.98H:6.88 N:3.73 in the para position 6 H O ##STR24## A 234°C. 337 nm (CHCl3) (ε = 38,700) Theory: C:83.54H:8.51 O:7.95Found:C:83.54H:8.56 O:7.91 in the para position 7 H O ##STR25## C 84°C 335 nm (CHCl3)(ε = 39,500) Theory: C:73.15 H:7.37Found:C:73.06 H:7.30 in the para position 8 H O CHCHCO2(CH2 )3CH3 B + E 80°C 331 nm (CHCl3) Theory: C:78.65 H:8.25 in the para position (ε = 43,500) Found:C:78.75 H:8.24 9 H O ##STR26## D 83°C 355 nm (CHCl3)(ε = 39,000) Theory: C:77.82H:8.33 N:3.13Found:C:77.83H:8.28 N:3.12 in the para position 10 H n = 4R2 = CH3 ##STR27## F 270°C 290 nm (CHCl3)(ε = 12,500) Theory: C:83.79 H:9.23Found:C:83.59 H:9.24 in the para position 11 H O ##STR28## C <55°C 332 nm (CHCl3)(ε = 39,000) Theory: C:78.05 H:9.27Found:C:78.01 H:9.29 in the para position 12 H O CHCHCONH2-ethylhexyl B + G + H <55°C 328 nm (CHCl3) Theory: C:79.76 in the para position (ε = 47,000) H:9.32 N:3.32 Found:C:79.69 H:9.35 N:3.25 13 H O ##STR29## B + G + I 144°C 328 nm (CHCl3)(ε = 47,800) Theory: C:78.11 H:7.02Found:C:78.35 H:7.06 in the para position 14 H O ##STR30## J 152°C 295 nm (CHCl3)(ε = 41,500) Theory: C:83.54 H:8.51Found:C:83.48 H:8.50 in the meta position 15 H O CHCHCOO(CH2)8CH B + K oil 329 nm (EtOH) Theory: C:81.38 H:10.08 CH(CH2)7CH3 (ε = 36,100) Found:C:81.16 H:10.19 in the para position 16 H O ##STR31## A Softening point134°C 208 nm (water)(ε = 37,000) Acid number:Theory: 2.07 meq/gFound:1.98 meq/g in the meta position 17 H O ##STR32## L 238°C 334 nm (EtOH)(ε = 32,750) Acid number:Theory: 2.59 meq/gFound: 2.56 meq/g in the para position 18 H O ##STR33## L + M 86°C 335 nm (EtOH)(ε = 40,000) Theory: C:81.66 H:8.14Found:C:81.34 H:8.27 in the para position 19 SO3 H O ##STR34## N 255°C with decomposition 342 nm (H2 O)(ε = 42,300) Theory: C:56.18 H:6.35O:26.76 S:10.70Found:C:55.92 H:6.40O:26.17 S:10.88 in the para position 20 SO3.crclbar. Na.sym. O ##STR35## N -- 345 nm (H2 O)(ε = 44,000) -- in the para position 21 SO3.crclbar. N.sym. H(CH2 CH2 OH)3 O ##STR36## N -- 345 nm (H2 O)(ε = 40,000) -- in the para position 22 H O ##STR37## O -106°C 323 nm (EtOH)(ε = 37,360) Theory: C:78.37 H:8.01Found:C:78.35 H:8.02 in the para position 23 H O CHCHCH2 ethyl P 85.5°C 283 nm (EtOH) Theory: C:78.07 H:7.74 in the para position (ε = 45,300) Found: C:78.04 H:7.72The procedures (A) to (P) used to prepare the compounds (1) to (23) are set out below.
134 g of 4'-formyl-3-benzylidene-camphor, 1,350 ml of dry toluene, 116 g of camphosulphonic acid and 22 g of sodium hydroxide pellets are placed in an equipped 3 liter three-necked round-bottomed flask. The mixture is heated under reflux for 1 hour, the water formed being separated off with the aid of a Dean-Stark apparatus (18 ml). The solution is cooled and poured into 3 liters of isopropyl ether. The precipitate is filtered off, washed with isopropyl ether and dried.
The compound obtained is dissolved in 2 liters of hot acetone and the solution is acidified with 25 ml of concentrated hydrochloric acid. The inorganic salts which precipitate are filtered off and the filtrate is evaporated to dryness. The residue is taken up in 1 liter of isopropyl ether, filtered off and dried in vacuo. This gives 191 g of compound (1) (yield=79%).
Compound (2) is obtained by neutralising an aqueous solution of compound (1) with triethanolamine used stoichiometric proportions. The aqueous solution is lyophilised to remove the water and to give the compound in powder form.
Procedure A is also used to prepare compound (6), the camphosulphonic acid being replaced by camphor, and to prepare compound (16), the 4'-formyl-3-benzylidene-camphor being replaced by 3'-formyl-3-benzylidene-camphor.
22 g of malonic acid and 40 ml of dry pyridine are placed in an equipped 250 ml round-bottomed flask. The mixture is stirred until dissolution is complete. 1 ml of piperidine is then added, followed by 27 g of 4'-formyl-3-benzylidene-camphor, and the whole is heated gradually to 110°C Gas is evolved and this stops after a heating time of about 1 hour 30 minutes.
The solution is then cooled and acidified by adding 100 ml of 6N hydrochloric acid. The precipitate formed is filtered off, washed with water until the washings are neutral, and dried in vacuo.
This gives 30 g of compound (4) (yield=96%).
69 g of 2-ethylhexyl malonate, 2 ml of piperidine, 500 ml of ethanol and 54 g of 4'-formyl-3-benzylidene-camphor are placed in an equipped 1 liter round-bottomed flask.
The mixture is heated under reflux for 24 hours. A further 2 ml of piperidine are then added and the mixture is heated under reflux for 6 hours.
The solution is cooled and concentrated in vacuo. The residue is taken up in 500 ml of toluene. The organic phase is washed several times with water, dried and concentrated in vacuo.
The oil obtained is chromatographed on silica (eluant: acetone/hexane (1/9)).
This gives 55 g of compound (3) (yield: 47%).
To prepare compounds (7) and (11), the 2-ethylhexyl malonate is replaced by ethyl malonate and menthyl malonate respectively.
10.6 ml of ethyl cyanoacetate, 50 ml of absolute ethanol and 1.5 g of potassium fluoride, as a catalyst, are placed in an equipped 250 ml round-bottomed flask.
27 g of 4'-formyl-3-benzylidene-camphor are added to this mixture in small portions. The reaction mixture becomes pasty, 125 ml of absolute ethanol are then introduced and the mixture is stirred at 50°C for 1 hour.
The mixture is cooled and the precipitate is filtered off, washed with 200 ml of ethanol and then with 200 ml of water and finally dried in vacuo.
This gives 32.7 g of compound (5) (yield: 90%).
To obtain compound (9), the ethyl cyanoacetate is replaced by 2'-ethylhexyl cyanoacetate.
56 g of p-(2-oxo-3-bornylidene-methyl)-cinnamic acid (compound 4), 27 g of butanol, 800 ml of dry benzene and 4 ml of concentrated sulphuric acid are placed in an equipped 2 liter reactor.
The mixture is heated under reflux for 4 hours, the water formed being separated off with the aid of a Dean-Stark apparatus.
The solution is then cooled and subsequently washed with water, dried and evaporated to dryness.
The residue is recrystallized from ethanol.
This gives 70 g of compound (8) (yield=76%).
40 g of camphor, 200 ml of dry toluene, 23 g of tetramethylterephthaldehyde and 9.6 g of sodium hydroxide pellets are placed in an equipped 1 liter reactor.
The mixture is heated under reflux for 96 hours, the water formed being separated off.
The organic phase is then washed with water, dried and concentrated in vacuo.
The residue is taken up in 500 ml of toluene and filtered off on silica. The solution is evaporated to dryness. This gives 21 g of compound (10) (yield=38%).
31 g of p-(2-oxo-3-bornylidene-methyl)-cinnamic acid (compound 4), 200 ml of dry toluene and 24 g of thionyl chloride are placed in an equipped 500 ml reactor.
The mixture is heated under reflux for 2 hours. The excess thionyl chloride is driven off and the toluene is then distilled in vacuo.
The residue is recrystallised from a 40/60 toluene/hexane mixture.
After drying, 26 g of p-(2-oxo-3-bornylidene-methyl)-cinnamoyl chloride are obtained (yield=80%).
10 g of the acid chloride obtained under G, 3.9 g of 2-ethylhexylamine, 4.2 ml of triethylamine and 100 ml of methylene chloride are placed in an equipped 250 ml round-bottomed flask.
The mixture is heated under reflux for 2 hours. After cooling, the organic phase is washed with water, dried and filtered and the filtrate is concentrated to dryness.
The oily residue is dried in vacuo to give an amorphous solid.
This gives 12.2 g of compound (12) (yield=96%).
4.15 g of p-methoxybenzyl alcohol and 20 ml of pyridine are placed in an equipped 100 ml round-bottomed flask, and 9.9 g of the acid chloride obtained under G are introduced in small portions at ambient temperature.
The reaction is slightly exothermic.
When the addition has ended, the mixture is heated at 70°C for 1 hour.
After cooling, the solution is poured into a mixture of 200 ml of ice and 30 ml of concentrated hydrochloric acid.
The precipitate formed is filtered off, washed with water and recrystallised from acetone. This gives 6.8 g of compound (13) (yield=52%).
25 g of potassium tert.-butylate and 250 ml of toluene are placed in an equipped one liter reactor, and 33.5 g of camphor are then introduced in small portions.
The reaction is exothermic (maximum temperature 60°C).
After the mixture has cooled to 40°C, a solution of 13.4 g of isophthaldehyde in 200 ml of dry toluene is introduced dropwise.
The mixture is then heated under reflux for about 4 hours and subsequently poured into 700 ml of ice containing 25 ml of concentrated hydrochloric acid. The solid formed is filtered off (isophthalic acid) and the filtrate is left to separate.
The organic phase is separated off, dried and concentrated in vacuo. The oily residue is chromatographed on a silica column (eluant=methylene chloride). This gives 10 g of compound (14).
300 ml of dry benzene, 200 ml of dry toluene, 228 g of oleyl alcohol, 3.2 ml of concentrated sulphuric acid and then 45 g of p-(2-oxo-3-bornylidene-methyl)-cinnamic acid (compound 4) are placed in an equipped 2 liter reactor.
The mixture is heated under reflux for 5 hours, the water formed being separated off with the aid of a Dean-Stark apparatus.
The solution is then cooled and is subsequently washed with water, dried and evaporated to dryness. The residue is subjected to distillation under 0.1 mm Hg at 160°-174°C in order to remove the excess oleyl alcohol. The expected ester is isolated by column chromatography in the presence of silica gel and chloroform (10 liters of CHCl3 +2 kg of silica gel).
The chloroform part, containing the oleyl p-(2-oxo-3-bornylidene-methyl)-cinnamate, is concentrated to give 40 g of compound (15) (yield 40%).
A mixture containing 17.4 g (0.1 mol) of potassium phenylacetate, 5 g (0.035 mol) of potassium carbonate, 0.5 ml of pyridine, 26.8 g (0.1 mol) of 4'-formyl-3-benzylidene-camphor and 15.3 g (0.15 mol) of acetic anhydride is heated for 2 hours at 180°-190°C A stream of nitrogen is maintained throughout the heating period.
After cooling, 300 ml of ice and then 50 ml of 6N potassium hydroxide solution are added. Extraction is carried out with 50 ml of ether and the aqueous phase is then acidified. The precipitate is recrystallized from 100 ml of 50% strength ethyl alcohol. This gives 15.2 g of compound (17).
A solution of 7.72 g (0.02 mol) of compound (17) obtained by procedure L, 5 ml of hexanol, 50 ml of toluene and 3 drops of concentrated sulphuric acid is heated under reflux in a round-bottomed flask equipped with a Dean-Stark apparatus.
After 3 hours under reflux, the reaction mixture is concentrated. The residue is recrystallized from ethanol. This gives 5.9 g of pale yellow product (18).
223 g (2 mols) of 97% strength sodium methylate are added to a suspension of 464.8 g (2 mols) of 10-d,l-camphosulphonic acid in 4 liters of toluene and 0.2 liter of methanol, and the mixture is then heated under reflux for 30 minutes.
A solution of 134.2 g (1 mol) of terephthalaldehyde in 1 liter of a 90/10 toluene/methanol mixture is then added in the course of 2 hours, under nitrogen. The mixture is kept under reflux for 1 hour and then cooled to ambient temperature.
The toluene is drawn off and the product is taken up in 1.5 liters of water and 1.5 liters of 35% strength hydrochloric acid. The mixture is heated under reflux for 1 hour, the residual toluene being distilled.
After the medium has been concentrated and cooled, the concentrate is filtered and the material on the filter is washed with 6N hydrochloric acid and dried in vacuo at 80°C and then at 100°C This gives 395 g of compound (19).
This is dissolved in water, the stoichiometric amount of sodium carbonate is added and the sodium disulphonate, which precipitates, is easily obtained. After dilution with acetone, filtration and drying in vacuo at 80°C and then at 100°C, the sodium disulphonate (20) is obtained with a virtually quantitative yield.
The triethanolamine salt (21) is obtained in the same way from compound (19) by using a stoichiometric amount of triethanolamine.
5 ml (10-2 mol) of ethyl 2-diethylphosphonopropionate, 5.4 g of 4'-formyl-3-benzylidene-camphor 2.10-2 mol), 40 ml of a saturated solution of potassium carbonate and 40 ml of water are introduced into a 250 ml round-bottomed flask. After vigorous stirring for 24 hours at ambient temperature, extraction is carried out with 3 times 50 ml of toluene. The organic phase is washed with water, distilled, dried and then evaporated to give 8 g of a yellowish oil, which crystallises in the cold. The product is recrystallized from hexane, which gives 5.2 g of white crystals of compound (22).
A suspension of 1 g of powdered potassium hydroxide in 30 ml of dioxane is placed in a 100 ml round-bottomed flask. A solution of 1.12 g (5.10-3 mol) of ethyl diethyl-phosphonoacetate and 1.34 g of 3'-formyl-3-benzylidene-camphor (5.10-3 mol) in 30 ml of dioxane is added dropwise. After stirring for 1 hour, the reaction medium is diluted with 40 ml of toluene. Filtration and evaporation of the solvents gives an oil, which crystallises in the cold. After recrystallisation from hexane, a product which melts at 85.5°C (23) is obtained.
The present invention also provides a cosmetic composition containing at least one 3-benzylidene-camphor derivative of the formula (I) according to the invention, as an agent for protection against ultraviolet rays, in a cosmetically acceptable medium.
If it is used as a composition intended for protecting the human epidermis against ultraviolet rays, the cosmetic composition according to the invention can be presented in the widest variety of forms normally used for this type of composition. It can be, in particular, in the form of a solution, a lotion, an emulsion such as a cream or a milk, an aqueous-alcoholic or alcoholic gel or a solid stick, or can be packaged in an aerosol.
It can contain the cosmetic adjuvants normally used in this type of composition, such as thickeners, softeners, humectants, superfatting agents, emollients, wetting agents, surface-active agents, preservatives, anti-foam agents, perfumes, oils, waxes, dyestuffs and/or pigments serving to colour the composition itself or the skin, bactericides or any other ingredient normally used in cosmetics.
The compound of the formula (I) is suitably present in proportions by weight of 0.5 to 15%, relative to the total weight of the composition.
Solubilisation solvents which can be used include a lower monoalcohol or polyol or a mixture thereof, or an aqueous-alcoholic solution. The particularly preferred monoalcohols or polyols are ethanol, isopropanol, propylene glycol and glycerol.
One embodiment of the invention is an emulsion in the form of a protective cream or milk comprising, in addition to a compound of the formula (I), at least one fatty alcohol, oxyethyleneated fatty alcohol or fatty acid ester, and, in particular, a fatty acid triglyceride, a fatty acid, lanoline, a natural or synthetic oil, or a wax, in the presence of water.
Another embodiment consists of lotions such as oily-alcoholic lotions based on a lower alcohol such as ethanol, or on a glycol such as propylene glycol, and/or on a polyol such as glycerol, and on a fatty acid ester such as a fatty acid triglyceride.
The cosmetic composition of the invention can also be an aqueous-alcoholic gel comprising one or more lower alcohols such as ethanol, propylene glycol or glycerol, and a thickener, in the presence of water.
The present invention also provides anti-sunburn cosmetic compositions containing at least one compound of the formula (I), which can be associated with other sun filters specific for UV-B radiation and/or UV-A radiation, which are compatible with the compounds according to the invention. It is thus possible to obtain a formulation which filters out all the UV-B and UV-A radiation.
The compounds according to the invention can be associated with UV-B filters which can be liposoluble compounds or oils having filtering properties, in particular coffee bean oil. Lipophilic UV-B sun filters which may be mentioned include salicyclic acid derivatives such as 2-ethylhexyl salicylate and homomenthyl salicylate, cinnamic acid derivatives such as 2-ethylhexyl p-methoxycinnamate and 2-ethoxyethyl p-methoxycinnamate, p-aminobenzoic acid derivatives such as amyl p-aminobenzoate and 2-ethylhexyl p-dimethylamino-benzoate, benzophenone derivatives such as 2-hydroxy-2-methoxybenzophenone and 2,2'-dihydroxy-4-methoxy-benzophenone, and camphor derivatives such as 3-(4-methylbenzylidene)-camphor, optionally associated with 4-isopropyldibenzoylmethane or 3-benzylidene-camphor.
As water-soluble sun filters which filter out the UV-B rays and which can also be associated with the liposoluble or water-soluble filters of the invention, provided that they are compatible with the latter, there may be mentioned the benzylidene-camphor derivatives described in French Pat. Nos. 2,199,971, 2,236,515, 2,383,904, and, more particularly, 4-(2-oxo-3-bornylidene-methyl)-phenyltrimethylammonium methylsulphate and salts of 4-(2-oxo-3-bornylidene-methyl)-benzenesulphonic acid, of 2-methyl-5-(2-oxo-3-bornylidene-methyl)-benzenesulphonic acid and of 2-phenylbenzimidazole-5-sulphonic acid.
The compounds according to the invention can also be associated with UV-A filters, amongst which dibenzoylmethane derivatives may be mentioned.
It is to be understood that the list of sun filters which can be used in association with the compounds (I) according to the invention is not exhaustive.
The anti-sunburn compositions according to the invention can be presented in the form of, for example, solutions, lotions, emulsions such as a cream or a milk, oils, fatty gels or aqueous-alcoholic or alcoholic gels, or can be packaged in an aerosol or as solid sticks. They can contain the abovementioned cosmetic adjuvants normally used in this type of composition.
The present invention also provides coloured or non-coloured cosmetic compositions containing at least one compound of the formula (I) as an agent for protection against ultraviolet rays.
These compositions may be in the form of, for example, hair compositions such as hair lacquers, setting lotions, which optionally have a treating or disentangling function, shampoos, colouring shampoos and hair dyeing compositions, make-up products such as nail varnishes, epidermis treatment creams, make-up foundations and lipsticks, and any other cosmetic composition which, by virtue of its constituents, can present problems of light stability during storage.
The invention also provides a process for protecting the human epidermis against UV-A rays and UV-B rays, which consists in applying, to the skin, at least one compound of the formula (I) in a cosmetically acceptable medium and optionally associated with other agents which absorb UV-A and/or UV-B rays.
The invention also provides a process for protecting coloured cosmetic compositions against UV-A and UV-B rays, which consists in incorporating at least one compound of the formula (I) into these compositions.
The present invention is further illustrated by the following application Examples.
| ______________________________________ |
| Protecting day cream |
| ______________________________________ |
| Compound of Example 7 1 g |
| Polyoxyethyleneated fatty alcohols |
| 7 g |
| Fatty acid triglycerides 30 g |
| Glycerol monostearate 2 g |
| Silicone oil 1.5 g |
| Cetyl alcohol 1.5 g |
| Preservatives 0.3 g |
| Perfume 0.6 g |
| Demineralised water q.s.p. |
| 100 g |
| ______________________________________ |
To prepare this cream, the fatty substances are heated to about 80°-85°C; the filter of the formula (I) is added. The water is heated separately to 80°-85°C and the fatty phase is added to the aqueous phase with vigorous stirring; the stirring is maintained for 10 to 15 minutes and the mixture is then left to cool, with moderate stirring, and the perfume is added at about 40°C
| ______________________________________ |
| Protecting day cream |
| ______________________________________ |
| Compound of Example 6 0.5 g |
| Benzylidene-camphor 0.5 g |
| Triglycerides of C8 to C12 fatty acids |
| 31 g |
| Glycerol monostearate 6 g |
| Stearic acid 2 g |
| Cetyl alcohol 1.2 g |
| Lanoline 4 g |
| Preservatives 0.3 g |
| Propanediol 2 g |
| Triethanolamine 0.5 g |
| Perfume 0.5 g |
| Demineralised water q.s.p. |
| 100 g |
| ______________________________________ |
The fatty substances are heated to about 80°-85°C and the filters are added; with vigorous stirring, the fatty phase is added to the water (containing the water-soluble compounds) heated to about 80°-85°C beforehand. After vigorous stirring for 15 minutes, the mixture is left to cool, with moderate stirring.
PAC Day creamThis composition is identical to that of Example 25, the compound of Example 6 being replaced by 0.8 g of the compound of Example 10.
| ______________________________________ |
| Protecting milk |
| ______________________________________ |
| Compound of Example 8 0.5 g |
| Octyl p-dimethylaminobenzoate |
| 0.5 g |
| Cetyl-stearyl alcohol 2 g |
| Cetyl alcohol 2 g |
| Triglycerides of C8 to C12 fatty acids |
| 20 g |
| Lanoline 4 g |
| Stearic acid 0.5 g |
| Preservatives 0.3 g |
| Carbopol 934 (crosslinked polyacrylic |
| 0.15 g |
| acid sold by GOODRICH CHEMICAL) |
| Triethanolamine 0.2 g |
| Perfume 0.4 g |
| Demineralised water q.s.p. |
| 100 g |
| ______________________________________ |
The emulsion is prepared in the same way as in Example 25.
| ______________________________________ |
| Oily-alcoholic sun lotion |
| ______________________________________ |
| Compound of Example 13 1.5 g |
| Perfume 0.5 g |
| 96° strength ethanol |
| 47.5 g |
| Triglycerides of C8 to C12 fatty acids q.s.p. |
| 100 g |
| 2-Ethylhexyl p-methoxycinnamate |
| 2 g |
| ______________________________________ |
The mixture of the various constituents is heated to about 40°-45°C in order to homogenise them and give a clear lotion.
| ______________________________________ |
| Sun cream |
| ______________________________________ |
| Compound of Example 8 3 g |
| 4-[(2-Oxo-3-bornylidene)-methyl]-phenyl- |
| 2.5 g |
| trimethylammonium methylsulphate |
| Polyoxyethyleneated fatty alcohols |
| 7 g |
| Triglycerides of C8 --C12 fatty acids |
| 30 g |
| Glycerol monostearate 2 g |
| Silicone oil 1.5 g |
| Cetyl alcohol 1.5 g |
| Preservatives 0.3 g |
| Perfume 0.6 g |
| Demineralised water q.s.p. |
| 100 g |
| ______________________________________ |
The preparation of this cream is similar to that of Example 24; in this case, the 4-[(2-oxo-3-bornylidene)-methyl]-phenyltrimethylammonium methylsulphate is dissolved in the water.
| ______________________________________ |
| Sun cream |
| ______________________________________ |
| Compound of Example 7 2.5 g |
| Benzylidene-camphor 4 g |
| Triglycerides of C8 to C12 fatty acids |
| 31 g |
| Glycerol monostearate 6 g |
| Stearic acid 2 g |
| Cetyl alcohol 1.2 g |
| Lanoline 4 g |
| Preservatives 0.3 g |
| Propanediol 2 g |
| Triethanolamine 0.5 g |
| Perfume 0.4 g |
| Demineralised water q.s.p. |
| 100 g |
| ______________________________________ |
The filters are dissolved in the fatty phase. The compound of Example 7 can be replaced by 2.5 g of the compound of Example 11.
PAC Sun oilThe following ingredients are mixed, if necessary with heating to 40°-45°C to homogenise them:
| ______________________________________ |
| Compound of Example 8 3 g |
| Octyl p-dimethylaminobenzoate |
| 3 g |
| Cacao butter 2.5 g |
| Antioxidants 0.05 g |
| Perfume 0.5 g |
| Triglycerides of C8 to C12 fatty acids q.s.p. |
| 100 g |
| ______________________________________ |
The compound of Example 8 can be replaced by 3 g of the compound of Example 9.
| ______________________________________ |
| Sun gel |
| ______________________________________ |
| Compound of Example 5 2.5 g |
| 2-Ethylhexyl p-methoxycinnamate |
| 2.5 g |
| Cacao butter 5 g |
| Antioxidants 0.05 g |
| Silica 10 g |
| Perfume 0.5 g |
| Triglycerides q.s.p. 100 g |
| ______________________________________ |
This fatty gel is prepared by heating the fatty substances to about 40°-45°C and then adding the silica, with vigorous stirring, and the filters.
The same results are obtained by replacing the compound of Example 5 by the compound of Example 3.
| ______________________________________ |
| Sun milk |
| ______________________________________ |
| Compound of Example 2 3 g |
| Compound of Example 14 2 g |
| Cetyl-stearyl alcohol 2 g |
| Cetyl alcohol 2 g |
| Triglycerides of C8 to C12 fatty acids |
| 20 g |
| Lanoline 4 g |
| Stearic acid 0.5 g |
| Preservatives 0.3 g |
| Carbopol 934 (crosslinked polyacrylic |
| 0.15 g |
| acid sold by GOODRICH CHEMICAL) |
| Triethanolamine 0.2 g |
| Demineralised water q.s.p. |
| 100 g |
| ______________________________________ |
This emulsion is prepared as in Example 25; the compound of Example 2 is dissolved in the aqueous phase, the compound of Example 14 being dissolved in the fatty phase.
| ______________________________________ |
| Aqueous-alcoholic sun gel |
| ______________________________________ |
| Carbopol 934 0.7 g |
| Triethanolamine 0.35 g |
| Propylene glycol 25 g |
| 96° strength ethanol |
| 25 g |
| Compound of Example 2 1 g |
| Diethanolamine salt of p-methoxycinnamic acid |
| 2.5 g |
| Preservative 0.3 g |
| Perfume 0.4 g |
| Demineralised water q.s.p. 100 g |
| ______________________________________ |
The carbopol is dispersed in the water with vigorous stirring and the triethanolamine is then added, followed by the solvents and the water, in which the filters have been dissolved beforehand.
The same results are obtained by replacing the compound of Example 2 by the compound of Example 4 in the form of the triethanolamine salt.
| ______________________________________ |
| Sun cream |
| ______________________________________ |
| Compound of Example 7 4 g |
| 4-[(2-Oxo-3-bornylidene)-methyl]-phenyl- |
| 3.5 g |
| trimethylammonium methylsulphate |
| 3.5 g |
| Polyoxyethyleneated fatty alcohols |
| 7 g |
| Triglycerides of C8 to C12 fatty acids |
| 30 g |
| Glycerol monostearate 2 g |
| Silicone oil 1.5 g |
| Cetyl alcohol 1.5 g |
| Preservatives, perfume q.s. |
| Demineralised water q.s.p. |
| 100 g |
| ______________________________________ |
The preparation of this cream is similar to that of Example 24, the 4-[(2-oxo-3-bornylidene)-methyl]-phenyl-trimethylammonium methylsulphate being dissolved in the water.
The compound of Example 7 can be replaced by 2 g of the compound of Example 12.
| ______________________________________ |
| Sun cream |
| ______________________________________ |
| Compound of Example 14 2 g |
| 4'-Methoxy-4-tert.-butyldibenzoylmethane sold |
| 1 g |
| under the name PARSOL 1789 by GIVAUDAN |
| Polyoxyethyleneated fatty alcohols |
| 7 g |
| Triglycerides of C8 to C12 fatty acids |
| 30 g |
| Glycerol monostearate 2 g |
| Silicone oil 1.5 g |
| Cetyl alcohol 1.5 g |
| Preservatives 0.4 g |
| Perfume 0.5 g |
| Demineralised water q.s.p. 100 g |
| ______________________________________ |
The compound of Example 14 and the Parsol 1789 are dissolved in the fatty phase.
In these examples, the compounds of the formula (I) are used to protect coloured compositions from the sun.
| ______________________________________ |
| Coloured Shampoo |
| ______________________________________ |
| Triethanolamine lauryl-sulphate |
| 10 g |
| 0.05% strength solution of Orasol Blue BLW |
| 1 cc |
| Compound of Example 2 0.5 g |
| Perfume, preservative q.s. |
| Water q.s.p. 100 g |
| ______________________________________ |
| ______________________________________ |
| Coloured shampoo |
| ______________________________________ |
| Triethanolamine lauryl-sulphate |
| 10 g |
| Compound of Example 1 0.8 g |
| Fast Lilac W 5001 (Colour Index No. 45190) |
| 0.015 g |
| Perfume, preservative q.s. |
| Water q.s.p. 100 g |
| ______________________________________ |
| ______________________________________ |
| Coloured setting lotion |
| ______________________________________ |
| Polyvinylpyrrolidone copolymer (of average |
| 2 g |
| molecular weight 40,000, sold under the code |
| K30 by GAF) |
| Fast Red CR1 W 3000 (Colour Index No. 27290) |
| 0.02 g |
| Compound of Example 3 0.3 g |
| 96° strength ethanol |
| 60 g |
| Water q.s.p. 100 g |
| ______________________________________ |
These compositions do not change colour, even after exposure to the sun for several weeks.
PAC Sun oilThe following ingredients are mixed, if necessary with heating to 40°-45°C to homogenise them:
| ______________________________________ |
| Compound of Example 15 3 g |
| Octyl p-dimethylaminobenzoate |
| 3 g |
| Cacao butter 2.5 g |
| Antioxidants 0.05 g |
| Perfume 0.5 g |
| Triglycerides of C8 to C12 fatty acids q.s.p. |
| 100 g |
| ______________________________________ |
| ______________________________________ |
| Aqueous-alcoholic sun gel |
| ______________________________________ |
| Carbopol 934 0.7 g |
| Triethanolamine 0.35 g |
| Propylene glycol 25 g |
| 96° strength ethanol |
| 25 g |
| Compound of Example 16 3 g |
| Preservative 0.3 g |
| Perfume 0.4 g |
| Demineralised water q.s.p. |
| 100 g |
| ______________________________________ |
The carbopol is dispersed in the water with vigorous stirring and the triethanolamine is then added, followed by the solvents and the water, in which the filter has been dissolved beforehand.
| ______________________________________ |
| Sun cream |
| ______________________________________ |
| Compound of Example 18 2.5 g |
| Benzylidene-camphor 4 g |
| Triglycerides of C8 to C12 fatty acids |
| 31 g |
| Glycerol monostearate 6 g |
| Stearic acid 2 g |
| Cetyl alcohol 1.2 g |
| Lanoline 4 g |
| Preservatives 0.3 g |
| Propanediol 2 g |
| Triethanolamine 0.5 g |
| Perfume 0.4 g |
| Demineralised water q.s.p. |
| 100 g |
| ______________________________________ |
The filters are dissolved in the fatty phase.
| ______________________________________ |
| Sun milk |
| ______________________________________ |
| Compound of Example 21 3 g |
| Benzylidene-camphor 2 g |
| Cetyl-stearyl alcohol 2 g |
| Cetyl alcohol 2 g |
| Triglycerides of C8 to C12 fatty acids |
| 20 g |
| Lanoline 4 g |
| Stearic acid 0.5 g |
| Preservatives 0.3 g |
| Carbopol 934 (crosslinked polyacrylic |
| 0.15 g |
| acid sold by GOODRICH CHEMICAL) |
| Triethanolamine 0.2 g |
| Demineralised water q.s.p. |
| 100 g |
| ______________________________________ |
This emulsion is prepared as in Example 33; the compound of Example 21 is dissolved in the aqueous phase, the benzylidene-camphor being dissolved in the fatty phase.
| ______________________________________ |
| Moisturising face cream |
| ______________________________________ |
| Tween 60 = sorbitan monostearate oxyethyleneated |
| 1 g |
| with 20 mols of ethylene oxide, sold by ATLAS |
| Cetyl alcohol 1 g |
| Perhydrosqualene 10 g |
| Virgin sesame oil 5 g |
| Stearic acid 2 g |
| Glycerol 3 g |
| Compound of Example 20 1 g |
| Methyl para-hydroxybenzoate |
| 0.3 g |
| Perfume 0.3 g |
| Water q.s.p. 100 g |
| ______________________________________ |
| ______________________________________ |
| Protecting and moisturising fluid body emulsion |
| ______________________________________ |
| Myrj 49 = polyethylene glycol stearate sold |
| 0.8 g |
| by ATLAS |
| Self-emulsifiable glycerol stearate |
| 1.2 g |
| Stearyl alcohol 1 g |
| Vaseline oil 8 g |
| Soya oil 3 g |
| Amerchol L 101 = extract of sterols and complex |
| 3 g |
| higher alcohols of lanoline, in their free form, |
| sold by AMERCHOL |
| Compound of Example 20 1.5 g |
| Methyl para-hydroxybenzoate |
| 0.3 g |
| Perfume 0.3 g |
| Water q.s.p. 100 g |
| ______________________________________ |
| ______________________________________ |
| Moisturising hand cream |
| ______________________________________ |
| Brij 56 = cetyl alcohol oxyethyleneated with |
| 2 g |
| 10 mols of ethylene oxide, sold by ATLAS |
| Self-emulsifiable glycerol stearate |
| 2 g |
| Cetyl alcohol 1 g |
| Vaseline oil 5 g |
| Isopropyl myristate 5 g |
| Lanoline 3 g |
| Compound of Example 20 2 g |
| Methyl para-hydroxybenzoate |
| 0.3 g |
| Perfume 0.3 g |
| Water q.s.p. 100 g |
| ______________________________________ |
| ______________________________________ |
| Stimulating cream |
| ______________________________________ |
| Germal 115 = imidazoline/urea copolymer sold |
| 0.3 g |
| by SUTTON LARS |
| Compound of Example 20 1 g |
| Omadine MDS = 2,2'-bis-N--hydroxypyridyl |
| 0.025 g |
| disulphide/magnesium sulphate complex sold by |
| OLIN |
| Triethanolamine 0.5 g |
| Cetiol LC = cetyl laurate sold by HENKEL |
| 1 g |
| Rutile titanium oxide 0.5 g |
| Triple pressed stearine 3 g |
| Mixture of glycerol monostearate and distearate |
| 3 g |
| Double-distilled pure cetyl alcohol |
| 3 g |
| Nesatol = triglycerides of C10 --C18 fatty |
| 1 g |
| acids, sold by VEVY |
| Calophyllum oil 0.5 g |
| BHA = butylhydroxyanisole 0.03 g |
| Nipa ester 82121 = mixture of methyl, ethyl, |
| 0.2 g |
| propyl, butyl and benzyl para-hydroxybenzoates |
| Talc 3 g |
| Octyl p-dimethylaminobenzoate |
| 1.5 g |
| Perfume 0.4 g |
| Demineralised water q.s.p. 100 g |
| ______________________________________ |
| ______________________________________ |
| Sun oil |
| ______________________________________ |
| Compound of Example 22 1.5 g |
| Compound of Example 23 1.5 g |
| Cacao butter 2.5 g |
| Antioxidants 0.05 g |
| Perfume 0.5 g |
| Triglycerides of C8 --C12 fatty acids q.s.p. |
| 100 g |
| ______________________________________ |
Leduc, Madeleine, Lang, Gerard, Malaval, Alain
| Patent | Priority | Assignee | Title |
| 4950478, | Jan 26 1983 | L'Oreal | Cosmetic compositions containing natural essences and benzylidenecamphor derivatives |
| 5064641, | Nov 22 1988 | L'Oreal | Polyvalent metal salts of sulphonted derivatives of benzylidenecamphor and their use for protecting the skin against ultraviolet radiation |
| 5762912, | Apr 19 1994 | L Oreal | H2 O-resistant sunscreen/cosmetic compositions comprising hydrophilic acidic species |
| 5938825, | May 21 1998 | TROY TECHNOLOGY CORPORATION, INC | Stabilized antimicrobial compositions containing halopropynyl compounds |
| 6042814, | Oct 16 1995 | SYMRISE GMBH & CO KG | Sulphonic acids and their use as UV absorbers |
| 6059991, | Dec 12 1997 | TROY TECHNOLOGY CORPORATION, INC | Stabilized composition containing halopropynyl compounds |
| 6353021, | Dec 12 1997 | Troy Technology Corporation, Inc. | Stabilized composition containing halopropynyl compounds |
| 6472424, | Jun 07 2000 | Troy Technology Corporation, Inc. | Stabilized antimicrobial compositions containing halopropynyl compounds and benzylidene camphors |
| 7074396, | Oct 22 2003 | Access Business Group International LLC | Composition and method for protecting both natural and artificial hair color from ultraviolet light damage |
| Patent | Priority | Assignee | Title |
| 4421739, | Mar 15 1977 | L'Oreal | Benzylidene-camphors, processes for their preparation and cosmetic compositions containing them |
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